Extending the solid solution range of sodium ferric pyrophosphate: Off-stoichiometric Na3Fe2.5(P2O7)2 as a novel cathode for sodium-ion batteries

Abstract

Iron-based pyrophosphates are attractive cathodes for sodium-ion batteries due to their large framework, cost-effectiveness, and high energy density. However, the understanding of the crystal structure is scarce and only a limited candidates have been reported so far. In this work, we found for the first time that a continuous solid solution, Na4−αFe2+α/2(P2O7)2 (0 ≤ α ≤ 1, could be obtained by mutual substitution of cations at center-symmetric Na3 and Na4 sites while keeping the crystal building blocks of anionic P2O7 unchanged. In particular, a novel off-stoichiometric Na3Fe2.5(P2O7)2 is thus proposed, and its structure, energy storage mechanism, and electrochemical performance are extensively investigated to unveil the structure–function relationship. The as-prepared off-stoichiometric electrode delivers appealing performance with a reversible discharge capacity of 83 mAh g−1, a working voltage of 2.9 V (vs. Na+/Na), the retention of 89.2% of the initial capacity after 500 cycles, and enhanced rate capability of 51 mAh g−1 at a current density of 1600 mA g−1. This research shows that sodium ferric pyrophosphate could form extended solid solution composition and promising phase is concealed in the range of Na4−αFe2+α/2(P2O7)2, offering more chances for exploration of new cathode materials for the construction of high-performance SIBs.